Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:108569572-108570008 | Common:3; Rare:159 | ||||
chr7:112206339-112206766 | Common:2; Rare:143 | ||||
chr7:112450235-112450465 | Common:4; Rare:72 | ||||
chr7:116524496-116525153 | Common:3; Rare:181; Clinvar (benign):2 | ||||
chr7:116526144-116526428 | Common:2; Rare:82 | ||||
chr7:116672191-116672468 | Common:1; Rare:63; Clinvar:2 | ||||
chr7:116953430-116953536 | Rare:42 | ||||
chr7:118183965-118184251 | Common:2; Rare:107 | ||||
chr7:121396224-121396499 | Common:1; Rare:91 | ||||
chr7:122144207-122144413 | Common:1; Rare:46 | ||||
chr7:123557773-123557956 | Common:1; Rare:49 | ||||
chr7:123748910-123749245 | Common:3; Rare:121 | ||||
chr7:124929785-124929884 | Common:2; Rare:27 | ||||
chr7:127392071-127392120 | Rare:21 | ||||
chr7:127651830-127652235 | Common:3; Rare:120 |